Canonical Allele Identifier: PA2826449699
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1163690
ClinVar RCV Id: RCV001508950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244917.1:p.Gly418Ala
CA412196844
NM_001257988.1:c.1253G>C